Aptamer-Based Electrochemical Microfluidic Biosensor for the Detection of Cryptosporidium parvum

微小隐孢子虫 适体 生物传感器 微流控 隐孢子虫 自来水 检出限 纳米技术 胶体金 化学 材料科学 色谱法 微生物学 生物 分子生物学 纳米颗粒 环境科学 粪便 环境工程
作者
Roozbeh Siavash Moakhar,Rohan Mahimkar,Arash Khorrami Jahromi,Sara Mahshid,Sahar Sadat Mahshid,Carolina del Real Mata,Yao Lü,Fabio Vasquez Camargo,Brent R. Dixon,John S. Gilleard,Alexandre J. da Silva,Momar Ndao,Sara Mahshid,Sara Mahshid
出处
期刊:ACS Sensors [American Chemical Society]
卷期号:8 (6): 2149-2158 被引量:34
标识
DOI:10.1021/acssensors.2c01349
摘要

Cryptosporidium parvum is a high-risk and opportunistic waterborne parasitic pathogen with highly infectious oocysts that can survive harsh environmental conditions for long periods. Current state-of-the-art methods are limited to lengthy imaging and antibody-based detection techniques that are slow, labor-intensive, and demand trained personnel. Therefore, the development of new sensing platforms for rapid and accurate identification at the point-of-care (POC) is essential to improve public health. Herein, we propose a novel electrochemical microfluidic aptasensor based on hierarchical 3D gold nano-/microislands (NMIs), functionalized with aptamers specific to C. parvum. We used aptamers as robust synthetic biorecognition elements with a remarkable ability to bind and discriminate among molecules to develop a highly selective biosensor. Also, the 3D gold NMIs feature a large active surface area that provides high sensitivity and a low limit of detection (LOD), especially when they are combined with aptamers,. The performance of the NMI aptasensor was assessed by testing the biosensor’s ability to detect different concentrations of C. parvum oocysts spiked in different sample matrices, i.e., buffer, tap water, and stool, within 40 min detection time. The electrochemical measurements showed an acceptable LOD of 5 oocysts mL–1 in buffer medium, as well as 10 oocysts mL–1 in stool and tap water media, over a wide linear range of 10–100,000 oocysts mL–1. Moreover, the NMI aptasensor recognized C. parvum oocysts with high selectivity while exhibiting no significant cross-reactivity to other related coccidian parasites. The specific feasibility of the aptasensor was further demonstrated by the detection of the target C. parvum in patient stool samples. Our assay showed coherent results with microscopy and real-time quantitative polymerase chain reaction, achieving high sensitivity and specificity with a significant signal difference (p < 0.001). Therefore, the proposed microfluidic electrochemical biosensor platform could be a stepping stone for the development of rapid and accurate detection of parasites at the POC.
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